Dual Elements Coupling Effect Induced Modification from the Surface into the Bulk Lattice for Ni-Rich Cathodes with Suppressed Capacity and Voltage Decay
Source abstract
Abstract
Injection of phase transition from a layered to rock-salt phase into the bulk lattice and side reactions on the interfacial usually causes structure degradation, quick capacity/voltage decay, and even thermal instability. Here, a self-formed interfacial protective layer coupled with lattice tuning was constructed for Ni-rich cathodes by simultaneous incorporation of Zr and Al in a one-step calcination. The migration energy between Zr and Al from the surface into the bulk lattice induces dual modifications from the surface into the bulk lattice, which effectively decrease the formation of cation mixing, the degree of anisotropic lattice change, and the generation of microcracks. With the stabilization role provided by the doped Zr-Al ions and protective function endowed by the surface layer, the modified cathode material exhibits significantly enhanced capacity and voltage retention. Specifically, the capacity retention for the modified cathode material reaches 99% after 100 cycles at 1 C and 25 °C in a voltage range of 3.0-4.3 V, which outperformed that for the pristine cathode (70%). The declination values of the average voltage for the modified cathode are only 0.025 and 0.097 V after 100 cycles at 1 C in voltage ranges of 3.0-4.3 and 2.8-4.5 V, respectively, which are much lower than those for the pristine cathode (0.230 and 0.405 V). The synchronous accomplishment of modification from the surface into the bulk lattice for Ni-rich materials with multiple elements in a one-step calcination process would provide some referenced value for the preparation of other cathode materials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Semiconductor materials and devices · Advanced Memory and Neural Computing
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemical Engineering, Sichuan University, Chengdu 610065, PR China
College of Materials and Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu 610059, PR China
Post-doctoral Mobile Research Center of Ruyuan Hec Technology Corporation, Ruyuan, Guangdong 512000, PR China
Institute for Applied Materials (IAM), Karlsruhe Institute of Technology (KIT), Eggenstein-Leopoldshafen 76344, Germany
Funding
Sichuan University · National Natural Science Foundation of China · Zigong City
References (49)
Show source-provided references
1. 10.1038/s41560-019-0409-z10.1038/s41560-019-0409-z ↗
2. 10.1021/jacs.8b0615010.1021/jacs.8b06150 ↗
3. 10.1021/acsenergylett.8b0249910.1021/acsenergylett.8b02499 ↗
4. 10.1021/jacs.8b1379810.1021/jacs.8b13798 ↗
5. 10.1038/s41560-018-0097-010.1038/s41560-018-0097-0 ↗
6. 10.1038/s41560-018-0191-310.1038/s41560-018-0191-3 ↗
7. 10.1021/acsenergylett.9b0073310.1021/acsenergylett.9b00733 ↗
8. 10.1016/j.nanoen.2019.10388710.1016/j.nanoen.2019.103887 ↗
9. 10.1021/acs.accounts.9b0003310.1021/acs.accounts.9b00033 ↗
10. 10.1038/ncomms1410110.1038/ncomms14101 ↗
11. 10.1016/j.electacta.2017.10.10110.1016/j.electacta.2017.10.101 ↗
12. 10.1002/aenm.20170361210.1002/aenm.201703612 ↗
13. 10.1002/aenm.20180120210.1002/aenm.201801202 ↗
14. 10.1002/aenm.20170178810.1002/aenm.201701788 ↗
15. 10.1016/j.electacta.2018.11.01010.1016/j.electacta.2018.11.010 ↗
16. 10.1016/j.ceramint.2015.02.02610.1016/j.ceramint.2015.02.026 ↗
17. 10.1002/aenm.20190153010.1002/aenm.201901530 ↗
18. 10.1021/acsenergylett.8b0230210.1021/acsenergylett.8b02302 ↗
19. 10.1002/aenm.20170251410.1002/aenm.201702514 ↗
20. 10.1016/j.jpowsour.2010.07.02110.1016/j.jpowsour.2010.07.021 ↗
21. 10.1016/j.jpowsour.2008.12.03710.1016/j.jpowsour.2008.12.037 ↗
22. 10.1021/acsenergylett.8b0080510.1021/acsenergylett.8b00805 ↗
23. 10.1021/acs.chemmater.7b0486110.1021/acs.chemmater.7b04861 ↗
24. 10.1149/2.0561701jes10.1149/2.0561701jes ↗
25. 10.1021/acs.jpcc.5b0685810.1021/acs.jpcc.5b06858 ↗
26. 10.1021/acsami.8b1037210.1021/acsami.8b10372 ↗
27. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
28. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
29. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
30. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
31. 10.1166/jnn.2018.1568610.1166/jnn.2018.15686 ↗
32. 10.1021/am506712c10.1021/am506712c ↗
33. 10.1016/j.jpowsour.2018.10.09410.1016/j.jpowsour.2018.10.094 ↗
34. 10.1039/C7SE00513J10.1039/C7SE00513J ↗
35. 10.1016/j.jpowsour.2016.07.00810.1016/j.jpowsour.2016.07.008 ↗
36. 10.1038/s41467-019-11299-210.1038/s41467-019-11299-2 ↗
37. 10.1016/j.electacta.2018.08.12410.1016/j.electacta.2018.08.124 ↗
38. 10.1021/acssuschemeng.7b0217810.1021/acssuschemeng.7b02178 ↗
39. 10.1002/smll.20180317910.1002/smll.201803179 ↗
40. 10.1002/aenm.20190115210.1002/aenm.201901152 ↗
41. 10.1002/aenm.20180029710.1002/aenm.201800297 ↗
42. 10.1021/acs.jpclett.7b0192710.1021/acs.jpclett.7b01927 ↗
43. 10.1002/aenm.20180390210.1002/aenm.201803902 ↗
44. 10.1021/acs.chemmater.7b0526910.1021/acs.chemmater.7b05269 ↗
45. 10.1002/anie.20190235910.1002/anie.201902359 ↗
46. 10.1016/j.nanoen.2018.04.06210.1016/j.nanoen.2018.04.062 ↗
47. 10.1039/C8NR01707G10.1039/C8NR01707G ↗
48. 10.1016/j.jpowsour.2017.11.02010.1016/j.jpowsour.2017.11.020 ↗
49. 10.1002/aenm.20170315410.1002/aenm.201703154 ↗